FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

SmartPerfusion

K Number: K181966 · Decision Aug 17, 2018
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
8
Review Days
25

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Basic Information

Device Name
SmartPerfusion
K Number
K181966
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems Nederlands B.V.
Date Received
July 23, 2018
Decision Date
August 17, 2018
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OWB Interventional Fluoroscopic X-Ray System

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